Valacyclovir Hydrochloride
- Product NDC
- 67296-1551
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valacyclovir Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA090682
- Marketing category
- ANDA
- Substance
- VALACYCLOVIR HYDROCHLORIDE
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 67296-1551-1 | 21 TABLET, FILM COATED in 1 BOTTLE (67296-1551-1) | 2019-10-30 | 0000-00-00 | No | Current |
| 67296-1551-5 | 5 TABLET, FILM COATED in 1 BOTTLE (67296-1551-5) | 2019-10-30 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| valacyclovir 1gm | RedPharm Drug, Inc. | 2024-08-26 | HUMAN PRESCRIPTION DRUG LABEL | 6 |